Canonical Allele Identifier: CA1182979092

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691195_97691196delinsAT , CM000663.2:g.97691195_97691196delinsAT	GRCh38
NC_000001.10:g.98156751_98156752delinsAT , CM000663.1:g.98156751_98156752delinsAT	GRCh37
NC_000001.9:g.97929339_97929340delinsAT	NCBI36
NG_008807.2:g.234864_234865delinsAT , LRG_722:g.234864_234865delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+521_762+522delinsAT MANE Select	ENSP00000359211.3:n.762+521_762+522delinsAT
ENST00000370192.7:c.762+521_762+522delinsAT	ENSP00000359211.3:n.762+521_762+522delinsAT
NM_000110.3:c.762+521_762+522delinsAT , LRG_722t1:c.762+521_762+522delinsAT	NP_000101.2:n.762+521_762+522delinsAT
XM_005270562.3:c.762+521_762+522delinsAT	XP_005270619.2:n.762+521_762+522delinsAT
XM_006710397.2:c.762+521_762+522delinsAT	XP_006710460.1:n.762+521_762+522delinsAT
XM_006710397.3:c.762+521_762+522delinsAT	XP_006710460.1:n.762+521_762+522delinsAT
XM_017000507.1:c.651+521_651+522delinsAT	XP_016855996.1:n.651+521_651+522delinsAT
XM_017000508.2:c.267+521_267+522delinsAT	XP_016855997.1:n.267+521_267+522delinsAT
XM_017000509.2:c.267+521_267+522delinsAT	XP_016855998.1:n.267+521_267+522delinsAT
XM_017000510.1:c.267+521_267+522delinsAT	XP_016855999.1:n.267+521_267+522delinsAT
NM_000110.4:c.762+521_762+522delinsAT MANE Select	NP_000101.2:n.762+521_762+522delinsAT